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Published on: May 15, 2019
Total synthesis of cribrostatin 6
Daniel Knueppel1, Stephen F Martin
1Department of Chemistry and Biochemistry, The University of Texas at Austin, 1 University Station-A5300, Austin, TX 78712-1167, USA.
Angewandte Chemie (International Ed. in English)
|February 25, 2009
Abstract:
Fast and furious: Cribrostatin 6, an antimicrobial and antineoplastic agent, was the target of a total synthesis where the longest linear sequence was only four steps. The key step involves a tandem 4pi electrocyclic ring opening, radical cyclization, and homolytic aromatic substitution sequence to afford the tricyclic core of the natural product.

